EUCTR2011-002508-34-ES进行中(未招募)不适用
Evaluate adherence to treatment with Glucophage sachets versus tablets in diabetes type 2 patients, previously treated with metformin tablets
MERCK, S.L.0 个研究点开始时间: 2011年10月13日最近更新:
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中(未招募)
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •- Type 2 Diabetes diagnosed. Baseline Glycaemia > 7,0 mmol/L (126 mg/dL) or overload Glycemia > 11,0 mmol/L (198 mg/dL)
- •- On treatment with metformin tablets
- •- To fulfill at any time at least one of the following criteria for cardio-vascular risk:
- •BP sistolic > 180 mmHg and/or >110 mmHg diastolic.
- •BP sistolic > 160 mmHg and <70 mmHg diastolic.
- •> 3 CV risk factors
- •Stablished CV disease or nephropathy
- •- Stablished dose of Metformin > 1.700 mg/day
- •- Age > 18 years old
- •- Given informed consent
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 140
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •- not able to take medication orally
- •- According to SmPC:
- •Known hypersensitivity to metformin or any of its excipients
- •Diabetic ketoacidosis or diabetic precoma in the previous week
- •Renal impairment or dysfunction (Creatinine clearance < 60 mL/min)
- •Acute disease which may produce renal dysfunction, tissue hypoxia as dehydration, severe infection, shock, administration of iodinated contrast.
- •Acute or chronic disease which may produce tissue hypoxia as cardiovascular or respiratory collapse, recent myocardial infarction, shock.
- •Liver impairment, alcohol poisoning o alcoholism
- •- Participating in other clinical trial in the 30 days prior to randomisation.
- •- Any other illnes or medical or psiquiatric condition, severe and uncontrolled that could interfere in the patient's participation or in the assesment of the study results.
研究者
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